[go: up one dir, main page]

PH12015501052A1 - Solid form of dihydro-pyrido-oxazine drivative - Google Patents

Solid form of dihydro-pyrido-oxazine drivative

Info

Publication number
PH12015501052A1
PH12015501052A1 PH12015501052A PH12015501052A PH12015501052A1 PH 12015501052 A1 PH12015501052 A1 PH 12015501052A1 PH 12015501052 A PH12015501052 A PH 12015501052A PH 12015501052 A PH12015501052 A PH 12015501052A PH 12015501052 A1 PH12015501052 A1 PH 12015501052A1
Authority
PH
Philippines
Prior art keywords
pyrido
dihydro
drivative
oxazine
solid form
Prior art date
Application number
PH12015501052A
Inventor
Hurth Konstanze
Kalis Christoph
Kammertoens Karen
Soldermann Nicolas
Zecri Frederic
Original Assignee
Novartis Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=51019963&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PH12015501052(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of PH12015501052A1 publication Critical patent/PH12015501052A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Epidemiology (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Dispersion Chemistry (AREA)
  • Nutrition Science (AREA)
  • Physiology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

The invention relates to an anhydrous crystalline form of (1,1-dioxo-hexahydro-1lambda*6*- thiopyran-4-yl)-{(S)-3-[1-(6-methoxy-5-methyl-pyridin-3-yl)-2,3-dihydro-1H-pyrido[3,4- b][1,4]oxazin-7-yloxy]-pyrrolidin-1-yl}-methanone; pharmaceutical compositions and combinations including these forms as well as to methods of using these forms, including their pharmaceutical compositions and combinations for the treatment of diseases.
PH12015501052A 2012-11-26 2015-05-12 Solid form of dihydro-pyrido-oxazine drivative PH12015501052A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GC201222895 2012-11-26
IR1391307213 2012-12-04
PCT/IB2013/060412 WO2014102630A1 (en) 2012-11-26 2013-11-26 Solid form of dihydro-pyrido-oxazine derivative

Publications (1)

Publication Number Publication Date
PH12015501052A1 true PH12015501052A1 (en) 2015-07-27

Family

ID=51019963

Family Applications (1)

Application Number Title Priority Date Filing Date
PH12015501052A PH12015501052A1 (en) 2012-11-26 2015-05-12 Solid form of dihydro-pyrido-oxazine drivative

Country Status (22)

Country Link
EP (1) EP2928896B1 (en)
KR (1) KR102184069B1 (en)
CN (1) CN104870451B (en)
AU (1) AU2013368997B8 (en)
BR (1) BR112015009870A2 (en)
CA (1) CA2891521A1 (en)
CL (1) CL2015001409A1 (en)
CY (1) CY1119702T1 (en)
DK (1) DK2928896T3 (en)
GT (1) GT201500124A (en)
IL (1) IL238889B (en)
MX (1) MX366342B (en)
NZ (1) NZ706865A (en)
PE (1) PE20150946A1 (en)
PH (1) PH12015501052A1 (en)
PL (1) PL2928896T3 (en)
PT (1) PT2928896T (en)
SG (1) SG11201503410VA (en)
TN (1) TN2015000128A1 (en)
TW (1) TW201422625A (en)
WO (1) WO2014102630A1 (en)
ZA (1) ZA201502350B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK2794600T3 (en) 2011-12-22 2018-03-12 Novartis Ag -2,3-Dihydro-benzo [1,4] oxazine derivatives and related compounds such as phosphoinositide 3-kinase (PI3K) inhibitors for the treatment of rheumatoid arthritis
HUE067912T2 (en) 2018-08-13 2024-11-28 Hoffmann La Roche New heterocyclic compounds as monoacylglycerol lipase inhibitors
CA3151516A1 (en) 2019-09-12 2021-03-18 F. Hoffmann-La Roche Ag 4,4a,5,7,8,8a-hexapyrido[4,3-b][1,4]oxazin-3-one compounds as magl inhibitors

Family Cites Families (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU11248A1 (en) 1927-03-29 1929-09-30 В.С. Григорьев Anthracene cleaning method
GB1524747A (en) 1976-05-11 1978-09-13 Ici Ltd Polypeptide
LU88769I2 (en) 1982-07-23 1996-11-05 Zeneca Ltd Bicalutamide and its pharmaceutically acceptable salts and esters (Casodex (R))
GB8327256D0 (en) 1983-10-12 1983-11-16 Ici Plc Steroid derivatives
US5093330A (en) 1987-06-15 1992-03-03 Ciba-Geigy Corporation Staurosporine derivatives substituted at methylamino nitrogen
US5010099A (en) 1989-08-11 1991-04-23 Harbor Branch Oceanographic Institution, Inc. Discodermolide compounds, compositions containing same and method of preparation and use
NZ243082A (en) 1991-06-28 1995-02-24 Ici Plc 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof
AU661533B2 (en) 1992-01-20 1995-07-27 Astrazeneca Ab Quinazoline derivatives
TW225528B (en) 1992-04-03 1994-06-21 Ciba Geigy Ag
GB9314893D0 (en) 1993-07-19 1993-09-01 Zeneca Ltd Quinazoline derivatives
ATE205483T1 (en) 1995-03-30 2001-09-15 Pfizer QUINAZOLINE DERIVATIVES
GB9508538D0 (en) 1995-04-27 1995-06-14 Zeneca Ltd Quinazoline derivatives
US5747498A (en) 1996-05-28 1998-05-05 Pfizer Inc. Alkynyl and azido-substituted 4-anilinoquinazolines
US5843901A (en) 1995-06-07 1998-12-01 Advanced Research & Technology Institute LHRH antagonist peptides
JP4146514B2 (en) 1995-07-06 2008-09-10 ノバルティス アクチエンゲゼルシャフト Pyrrolopyrimidines and process for producing the same
US5760041A (en) 1996-02-05 1998-06-02 American Cyanamid Company 4-aminoquinazoline EGFR Inhibitors
GB9603095D0 (en) 1996-02-14 1996-04-10 Zeneca Ltd Quinazoline derivatives
ES2174250T5 (en) 1996-04-12 2010-04-21 Warner-Lambert Company Llc IRREVERSIBLE THYROSINE KINASE INHIBITORS.
AU2912997A (en) 1996-06-24 1998-01-14 Pfizer Inc. Phenylamino-substituted tricyclic derivatives for treatment of hyperproliferative diseases
WO1998008849A1 (en) 1996-08-30 1998-03-05 Novartis Aktiengesellschaft Method for producing epothilones, and intermediate products obtained during the production process
CA2264908C (en) 1996-09-06 2006-04-25 Obducat Ab Method for anisotropic etching of structures in conducting materials
WO1998010767A2 (en) 1996-09-13 1998-03-19 Sugen, Inc. Use of quinazoline derivatives for the manufacture of a medicament in the treatment of hyperproliferative skin disorders
EP0837063A1 (en) 1996-10-17 1998-04-22 Pfizer Inc. 4-Aminoquinazoline derivatives
PL193229B1 (en) 1996-11-18 2007-01-31 F Biotechnologische Forschung Epothylones c,d,e & f, method of obtaining them and their application as a cytostatic agents as wel as plant protection products
US6441186B1 (en) 1996-12-13 2002-08-27 The Scripps Research Institute Epothilone analogs
CO4940418A1 (en) 1997-07-18 2000-07-24 Novartis Ag MODIFICATION OF A CRYSTAL OF A DERIVATIVE OF N-PHENYL-2-PIRIMIDINAMINE, PROCESSES FOR ITS MANUFACTURE AND USE
GB9721069D0 (en) 1997-10-03 1997-12-03 Pharmacia & Upjohn Spa Polymeric derivatives of camptothecin
US6194181B1 (en) 1998-02-19 2001-02-27 Novartis Ag Fermentative preparation process for and crystal forms of cytostatics
MXPA00008365A (en) 1998-02-25 2002-11-07 Sloan Kettering Inst Cancer Synthesis of epothilones, intermediates thereto and analogues therof.
ATE459616T1 (en) 1998-08-11 2010-03-15 Novartis Ag ISOCHINOLINE DERIVATIVES WITH ANGIOGENESIS-INHIBITING EFFECT
EP1135470A2 (en) 1998-11-20 2001-09-26 Kosan Biosciences, Inc. Recombinant methods and materials for producing epothilone and epothilone derivatives
PE20020354A1 (en) 2000-09-01 2002-06-12 Novartis Ag HYDROXAMATE COMPOUNDS AS HISTONE-DESACETILASE (HDA) INHIBITORS
BRPI0115193B1 (en) 2000-11-07 2016-08-09 Novartis Ag indolylmaleimide derivatives, process for preparing them as well as pharmaceutical composition comprising them
AR035885A1 (en) 2001-05-14 2004-07-21 Novartis Ag DERIVATIVES OF 4-AMINO-5-FENIL-7-CYCLLOBUTILPIRROLO (2,3-D) PYRIMIDINE, A PROCESS FOR ITS PREPARATION, A PHARMACEUTICAL COMPOSITION AND THE USE OF SUCH DERIVATIVES FOR THE PREPARATION OF A PHARMACEUTICAL COMPOSITION
GB0119249D0 (en) 2001-08-07 2001-10-03 Novartis Ag Organic compounds
AR039209A1 (en) 2002-04-03 2005-02-09 Novartis Ag INDOLILMALEIMIDA DERIVATIVES
BR0317099A (en) 2002-12-09 2005-10-25 Boardd Of Regents Of The Unive In vitro method to inhibit the function and / or proliferation of a janus tyrosine kinase 3, in vitro test method to assist in the identification of substances that are useful as therapeutic immunosuppressants, in vitro method to assist in the identification of a new immunosuppressant drug, in vitro to inhibit the function and / or proliferation of a cell expressing janus tyrosine kinase 3, use of at least one compound, isolated or purified chemical compound and pharmaceutical composition
KR101164541B1 (en) 2004-01-12 2012-07-10 와이엠 바이오사이언시즈 오스트레일리아 피티와이 엘티디 Selective kinase inhibitors
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
CN101300047A (en) * 2005-09-07 2008-11-05 雪兰诺实验室有限公司 PI3K inhibitors for the treatment of endometriosis
GB0620059D0 (en) * 2006-10-10 2006-11-22 Ucb Sa Therapeutic agents
DK2794600T3 (en) 2011-12-22 2018-03-12 Novartis Ag -2,3-Dihydro-benzo [1,4] oxazine derivatives and related compounds such as phosphoinositide 3-kinase (PI3K) inhibitors for the treatment of rheumatoid arthritis

Also Published As

Publication number Publication date
KR20150091047A (en) 2015-08-07
CA2891521A1 (en) 2014-07-03
AU2013368997B8 (en) 2015-10-08
IL238889B (en) 2021-03-25
NZ706865A (en) 2016-04-29
PL2928896T3 (en) 2018-01-31
CL2015001409A1 (en) 2015-07-24
TN2015000128A1 (en) 2016-10-03
EP2928896B1 (en) 2017-07-19
BR112015009870A2 (en) 2017-12-05
KR102184069B1 (en) 2020-11-30
PT2928896T (en) 2017-10-25
DK2928896T3 (en) 2017-11-06
IL238889A0 (en) 2015-07-30
AU2013368997A8 (en) 2015-10-08
HK1209419A1 (en) 2016-04-01
AU2013368997B2 (en) 2015-09-24
GT201500124A (en) 2016-03-01
WO2014102630A1 (en) 2014-07-03
ZA201502350B (en) 2017-08-30
SG11201503410VA (en) 2015-05-28
CN104870451B (en) 2017-07-07
PE20150946A1 (en) 2015-06-28
MX2015006650A (en) 2015-08-10
MX366342B (en) 2019-07-05
AU2013368997A1 (en) 2015-04-30
CN104870451A (en) 2015-08-26
EP2928896A1 (en) 2015-10-14
TW201422625A (en) 2014-06-16
CY1119702T1 (en) 2018-06-27

Similar Documents

Publication Publication Date Title
CA2871471C (en) Dna-pk inhibitors
UY32968A (en) FUSIONED HETEROCYCLIC COMPOUNDS AS OREXINE RECEIVER MODULATORS
MY193728A (en) Muscarinic receptor agonists
MX347917B (en) Imidazo [1, 2 - b] pyridazine - based compounds, compositions comprising them, and uses thereof.
MX346375B (en) Spiro-oxindole mdm2 antagonists.
IN2014CN03597A (en)
PH12015500376A1 (en) Novel bicyclic pyridinones
MX2013012652A (en) Derivatives of n- [(1h-pyrazol-1-yl) aryl] - 1h - indole or 1h - indazole - 3 - carboxamide, their preparation and their use as p2y12 antagonists.
MX2016007128A (en) Ccr6 compounds.
MX2014000964A (en) Substituted heterocyclic aza derivatives.
MY191352A (en) Aldosterone synthase inhibitors
PH12017500595A1 (en) Aldosterone synthase inhibitors
IN2012DN03846A (en)
PH12015501052A1 (en) Solid form of dihydro-pyrido-oxazine drivative
GB201209015D0 (en) Novel compounds
UA103197C2 (en) Use of nifurtimox for the treatment of diseases caused by trichomonadida
MX2015005312A (en) 1 h-indole-3-carboxamide derivatives and use thereof as p2y12 antagonists.
PH12014502780A1 (en) Azetidine and piperidine compounds useful as pde10 inhibitors
EA201591023A1 (en) SOLID FORM OF DERIVATIVE DIHYDROPYRIDOOXAZINE
PH12016502133A1 (en) Substituted tricycle compounds as fgfr inhibitors
MX2014002343A (en) Parp inhibitors.